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dbVar

Database of genomic structural variation

nsv5641455

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 129 SVs from 23 studies. See in: genome view

Submitted genomic98,988,746-98,988,746

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5641455	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	98,988,746	98,988,746
nsv5641455	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	98,324,450	98,324,450

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17141097	insertion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17141097	Submitted genomic		NC_000005.10:g.989 88746_98988747ins1 14	GRCh38 (hg38)		NC_000005.10	Chr5	98,988,746	98,988,746
nssv17141097	Remapped	Perfect	NC_000005.9:g.9832 4450_98324451ins11 4	GRCh37.p13	First Pass	NC_000005.9	Chr5	98,324,450	98,324,450

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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